RsmA (for regulator of secondary metabolism), RsmC, and rsmB RNA, the components of a posttranscriptional regulatory system, control extracellular protein production and pathogenicity in Erwinia carotovora subsp. carotovora. RsmA, an RNA binding protein, acts as a negative regulator by promoting message decay. rsmB RNA, on the other hand, acts as a positive regulator by neutralizing the effect of RsmA. RsmC modulates the levels of RsmA and rsmB RNA by positively regulating rsmA and negatively controlling rsmB. The level of rsmB RNA is substantially higher in RsmA ؉ bacteria than in RsmA ؊ mutants. We show that rsmB RNA is more stable in the presence of RsmA than in its absence. RsmA does not stimulate the expression of an rsmB-lacZ transcriptional fusion; in fact, the -galactosidase level is somewhat higher in RsmA ؊ bacteria than in RsmA Rsm (for regulator of secondary metabolism) is a novel type of posttranscriptional regulatory system which has a profound effect on bacterial metabolism and behavior. Rsm of Erwinia carotovora subsp. carotovora consists of three major components: an RNA binding protein, RsmA, which promotes RNA decay (8, 11); an untranslated RNA molecule, rsmB, which neutralizes RsmA action, apparently by sequestering RsmA (29); and RsmC, which positively regulates rsmA and negatively controls rsmB RNA levels (13). It is now apparent that Rsm and Rsm-like systems control diverse phenotypes in many prokaryotic species. In Erwinia, this regulatory system plays a critical role by affecting plant interaction, extracellular enzyme production, extracellular polysaccharide synthesis, swarming motility, secondary metabolite production, and the quorumsensing system (8,11,12,31,34,35). In Escherichia coli, a homologous system comprising CsrA (equivalent to RsmA) and csrB (equivalent to rsmB) RNA, controls glycogen synthesis, metabolism of acetate, motility and flagellum biosynthesis, and biofilm formation (21,27,40). There are substantial data indicating the existence of the regulatory system in various enterobacterial species, including human pathogens (2,3,5,9,14,40). Moreover, recent studies of several Pseudomonas species have demonstrated that RsmA-rsmB regulatory systems control secondary metabolite production and plant interaction.For example, in Pseudomonas aeruginosa, overexpression of rsmA reduces the levels of protease (Prt), elastase, and staphylolytic (LasA Prt) activity, as well as those of the PA-IL lectin, hydrogen cyanide, and pyocyanin. In Pseudomonas fluorescens, overexpressed prrB, which is structurally similar to rsmB, increases the production of Phl (2,4-diacetylphloroglucinol) and hydrogen cyanide (1,6,7,38). In Pseudomonas syringae pv. tomato strain DC3000, RsmA reduces the production of extracellular proteins, causes attenuation of pathogenicity in Arabidopsis thaliana, and lowers the efficiency of the induction of the hypersensitive reaction in tobacco